甲烷在M(1)-Ni(5)/SBA-15(M=Tb、Pr、Eu和Dy)催化剂上部分氧化制备清洁能源的氢气

H. Seo
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The active sites of the catalyst are verified through instrumental analysis with XPS, FETEM, and EDS.Results and Discussion : The XPS results show that when 1wt% of Eu is added to the Ni(5)/SBA-15 catalyst, the atomic percent of Ni2p3/2 is increased from 0.12% to 0.15%, and the oxygen atomic number including lattice oxygen and oxygen vacancies is increased 1.32 times compared to that of the Ni(5)/SBA-15 catalyst. Further, the O1s characteristic peak is chemically shifted toward the lower binding energy. The FETEM images show that the nanoparticles of Ni and Eu are uniformly distributed on the surface of a reduced Eu(1)-Ni(5)/SBA-15 catalyst. The EDS mappings of Eu, Ni, O, and Si are confirmed. It is believed that the activity of the catalyst was improved by increasing the dispersion of nanoparticles of Ni0 on the surface of the catalyst due to the increased mobility of oxygen by creating oxygen vacancies. Methane conversion of Ni(5)/SBA-15 catalyst was deactivated rapidly after the reaction time of 12h whereas M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu, and Dy) catalyst showed constant and stable catalyst activity until 12h ~ 50h. It is also considered to be the case that the sintering of Ni particles is prevented by the strong metal support interaction (SMSI) effect between Eu3+, Ni2+, and the SBA-15 carrier, and the stability of the catalyst is thereby maintained. The hydrogen yield of catalyst was in the order of Eu(1)-Ni(5)/SBA-15(57.2%, 25h) >> Dy(1)-Ni(5)/SBA-15 (49%, 14h) > Pr(1)-Ni(5)/SBA-15 (43.1%, 29h) > Tb(1)-Ni(5)/SBA-15 (42.8%, 25h).Conclusion : The Ni(5)/SBA-15 catalyst was showed that the conversion of methane was rapidly reduced after a reaction time of 12h, while when 1wt% of lanthanum (Tb, Pr, Eu and Dy) as a promoter was added to the Ni(5)/SBA-15 catalyst, the conversion of methane and yields of hydrogen were showed constant and stable catalytic activity in the reaction time of 12h to 50h. It is believed that the conversion of methane was improved by increasing the dispersion of nanoparticles of Ni0 on the surface of the catalyst due to the increased mobility of oxygen by creating oxygen vacancies. 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The active sites of the catalyst are verified through instrumental analysis with XPS, FETEM, and EDS.Results and Discussion : The XPS results show that when 1wt% of Eu is added to the Ni(5)/SBA-15 catalyst, the atomic percent of Ni2p3/2 is increased from 0.12% to 0.15%, and the oxygen atomic number including lattice oxygen and oxygen vacancies is increased 1.32 times compared to that of the Ni(5)/SBA-15 catalyst. Further, the O1s characteristic peak is chemically shifted toward the lower binding energy. The FETEM images show that the nanoparticles of Ni and Eu are uniformly distributed on the surface of a reduced Eu(1)-Ni(5)/SBA-15 catalyst. The EDS mappings of Eu, Ni, O, and Si are confirmed. It is believed that the activity of the catalyst was improved by increasing the dispersion of nanoparticles of Ni0 on the surface of the catalyst due to the increased mobility of oxygen by creating oxygen vacancies. 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引用次数: 0

摘要

目的:为了解决导致全球温室效应的环境问题,我们想评估1wt%的镧(Tb、Pr、Eu和Dy)作为促进剂添加到Ni(5)/SBA-15催化剂中,通过对天然气的主要成分甲烷进行部分氧化,在M(1)-Ni(5)/SBA-15(M=Tb、Pr、Eu和Dy)催化剂上转化为氢气,方法:在常压下,使用固定床流动反应器研究了M(1)-Ni(5)/SBA-15(M=Tb,Pr,Eu和Dy)催化剂上甲烷(POM)部分氧化为清洁能源氢气的催化活性。通过XPS、FETEM和EDS的仪器分析验证了催化剂的活性位点。结果与讨论:XPS结果表明,当向Ni(5)/SBA-15催化剂中加入1wt%的Eu时,Ni2p3/2的原子百分比从0.12%增加到0.15%,与Ni(5)/SBA-15催化剂相比,包括晶格氧和氧空位的氧原子序数增加了1.32倍。此外,O1s特征峰向较低的结合能发生化学位移。FETEM图像显示,Ni和Eu的纳米颗粒均匀分布在还原的Eu(1)-Ni(5)/SBA-15催化剂表面。证实了Eu、Ni、O和Si的EDS图谱。据信,由于通过产生氧空位增加了氧的迁移率,因此通过增加Ni0纳米颗粒在催化剂表面上的分散度来提高催化剂的活性。Ni(5)/SBA-15催化剂的甲烷转化在反应12h后迅速失活,而M(1)-Ni(5)/STBA-15(M=Tb、Pr、Eu和Dy)催化剂在反应12h~50h前表现出稳定的催化剂活性。还认为,通过Eu3+、Ni2+和SBA-15载体之间的强金属-载体相互作用(SMSI)效应来防止Ni颗粒的烧结,从而保持催化剂的稳定性。催化剂的氢气产率依次为Eu(1)-Ni(5)/SBA-15(57.2%,25h)>>Dy(1,当在Ni(5)/SBA-15催化剂中加入1wt%的镧(Tb、Pr、Eu和Dy)作为助催化剂时,在12h至50h的反应时间内,甲烷的转化率和氢气的产率显示出稳定的催化活性。据信,甲烷的转化率是通过增加Ni0纳米颗粒在催化剂表面的分散来提高的,这是由于通过产生氧空位增加了氧的迁移率。此外,强金属-载体相互作用(SMSI)效应阻止了Ni0纳米颗粒在M(1)-Ni(5)/SBA-15(M=Tb,Pr,Eu,Dy)催化剂表面的烧结。
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Hydrogen Production of Clean Energy by Partial Oxidation of Methane over M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu, and Dy) Catalysts
Objectives : In order to solve the environmental problem that is the cause of the global greenhouse effect, We want to evaluate the effects of 1wt% of lanthanum (Tb, Pr, Eu, and Dy) as a promoter added to Ni(5)/SBA-15 catalyst by performing the partial oxidation of methane, the main component of natural gas, to hydrogen over M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu and Dy) catalyst and to identify the active site of the catalyst by means of instrumentation such as XPS, FETEM, and EDS.Methods : The catalytic activities of the partial oxidation of methane (POM) to hydrogen as a clean energy over M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu, and Dy) catalysts are investigated using a fixed bed flow reactor under atmospheric pressure. The active sites of the catalyst are verified through instrumental analysis with XPS, FETEM, and EDS.Results and Discussion : The XPS results show that when 1wt% of Eu is added to the Ni(5)/SBA-15 catalyst, the atomic percent of Ni2p3/2 is increased from 0.12% to 0.15%, and the oxygen atomic number including lattice oxygen and oxygen vacancies is increased 1.32 times compared to that of the Ni(5)/SBA-15 catalyst. Further, the O1s characteristic peak is chemically shifted toward the lower binding energy. The FETEM images show that the nanoparticles of Ni and Eu are uniformly distributed on the surface of a reduced Eu(1)-Ni(5)/SBA-15 catalyst. The EDS mappings of Eu, Ni, O, and Si are confirmed. It is believed that the activity of the catalyst was improved by increasing the dispersion of nanoparticles of Ni0 on the surface of the catalyst due to the increased mobility of oxygen by creating oxygen vacancies. Methane conversion of Ni(5)/SBA-15 catalyst was deactivated rapidly after the reaction time of 12h whereas M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu, and Dy) catalyst showed constant and stable catalyst activity until 12h ~ 50h. It is also considered to be the case that the sintering of Ni particles is prevented by the strong metal support interaction (SMSI) effect between Eu3+, Ni2+, and the SBA-15 carrier, and the stability of the catalyst is thereby maintained. The hydrogen yield of catalyst was in the order of Eu(1)-Ni(5)/SBA-15(57.2%, 25h) >> Dy(1)-Ni(5)/SBA-15 (49%, 14h) > Pr(1)-Ni(5)/SBA-15 (43.1%, 29h) > Tb(1)-Ni(5)/SBA-15 (42.8%, 25h).Conclusion : The Ni(5)/SBA-15 catalyst was showed that the conversion of methane was rapidly reduced after a reaction time of 12h, while when 1wt% of lanthanum (Tb, Pr, Eu and Dy) as a promoter was added to the Ni(5)/SBA-15 catalyst, the conversion of methane and yields of hydrogen were showed constant and stable catalytic activity in the reaction time of 12h to 50h. It is believed that the conversion of methane was improved by increasing the dispersion of nanoparticles of Ni0 on the surface of the catalyst due to the increased mobility of oxygen by creating oxygen vacancies. Moreover, sintering of Ni0 nanoparticles on the surface of M(1)-Ni(5)/SBA-15 (M = Tb, Pr, Eu, Dy) catalyst is prevented by strong metal support interaction (SMSI) effect.
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